A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595995



Internal ID16383404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:162347904..162401249hg38UCSC Ensembl
Innerchr4:163269056..163322401hg19UCSC Ensembl
Innerchr4:163488506..163541851hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3853346
hg1953346
hg1853346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9363n54
Supporting Variantsnssv1010518
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595995
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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